Search Results - "Dávila Saldaña, Blachy J"
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Experience with a Reduced Toxicity Allogeneic Transplant Regimen for Non-CGD Primary Immune Deficiencies Requiring Myeloablation
Published in Journal of clinical immunology (01-01-2021)“…Purpose A need exists for reduced toxicity conditioning regimens that offer less toxicity while maintaining myeloablation, especially for primary immune…”
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Risk Factors for Symptomatic Pericardial Effusions Posthematopoietic Stem Cell Transplant
Published in Journal of transplantation (08-02-2023)“…Background. Pericardial effusions are a known complication posthematopoietic stem cell transplant (HSCT), causing significant morbidity. We aimed to evaluate…”
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Thymic Epithelial Cell Alterations and Defective Thymopoiesis Lead to Central and Peripheral Tolerance Perturbation in MHCII Deficiency
Published in Frontiers in immunology (15-06-2021)“…Major Histocompatibility Complex (MHC) class II (MHCII) deficiency (MHCII-D), also known as Bare Lymphocyte Syndrome (BLS), is a rare combined immunodeficiency…”
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Hospital survival following pediatric HSCT: changes in complications, ICU therapies and outcomes over 10 years
Published in Frontiers in pediatrics (12-10-2023)“…Hematopoietic stem cell transplantation (HSCT) is an increasingly utilized therapy for malignant and non-malignant pediatric diseases. HSCT complications,…”
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Pediatric lymphoproliferative disorders associated with inborn errors of immunity
Published in Clinical immunology (Orlando, Fla.) (01-09-2024)“…Both non-malignant and malignant lymphoproliferative disorders (LPD) are commonly seen in patients with inborn errors of immunity (IEI), which may be the…”
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High risk of relapsed disease in patients with NK/T-cell chronic active Epstein-Barr virus disease outside of Asia
Published in Blood advances (25-01-2022)“…Chronic active Epstein-Barr virus (EBV) disease (CAEBV) is characterized by high levels of EBV predominantly in T and/or natural killer cells with…”
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The genetic landscape of severe combined immunodeficiency in the United States and Canada in the current era (2010-2018)
Published in Journal of allergy and clinical immunology (01-01-2019)“…To the Editor: There has been increased appreciation in recent years that severe combined immunodeficiency (SCID) is not one disease, but rather a collection…”
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Poor T-cell receptor β repertoire diversity early posttransplant for severe combined immunodeficiency predicts failure of immune reconstitution
Published in Journal of allergy and clinical immunology (01-03-2022)“…Development of a diverse T-cell receptor β (TRB) repertoire is associated with immune recovery following hematopoietic cell transplantation (HCT) for severe…”
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Allogeneic hematopoietic cell transplantation is effective for p47phox chronic granulomatous disease: A Primary Immune Deficiency Treatment Consortium study
Published in Journal of allergy and clinical immunology (01-05-2024)“…P47phox (neutrophil cytosolic factor-1) deficiency is the most common cause of autosomal recessive chronic granulomatous disease (CGD) and is considered to be…”
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Tap water: A possible source of nontuberculous mycobacterial infection in patients with T cell deficiency
Published in American journal of infection control (01-07-2019)“…•Nontuberculous mycobacteria are an infectious threat to patients with lymphopenia.•Tap water is a potential source of infection, both in the community and the…”
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Primary Immunodeficiencies and Hematologic Malignancies: A Diagnostic Approach
Published in Frontiers in immunology (18-03-2022)Get full text
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B-cell differentiation and IL-21 response in IL2RG/JAK3 SCID patients after hematopoietic stem cell transplantation
Published in Blood (28-06-2018)“…Allogeneic hematopoietic stem cell transplant (HSCT) typically results in donor T-cell engraftment and function in patients with severe combined…”
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Haploidentical bone marrow transplantation in patients with relapsed or refractory severe aplastic anaemia in the USA (BMT CTN 1502): a multicentre, single-arm, phase 2 trial
Published in The Lancet. Haematology (01-09-2022)“…Relapsed severe aplastic anaemia is a marrow failure disorder with high morbidity and mortality. It is often treated with bone marrow transplantation at…”
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Aberrant T-cell exhaustion in severe combined immunodeficiency survivors with poor T-cell reconstitution after transplantation
Published in Journal of allergy and clinical immunology (01-01-2023)“…Severe combined immunodeficiency (SCID) comprises rare inherited disorders of immunity that require definitive treatment through hematopoietic cell…”
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SCID genotype and 6-month posttransplant CD4 count predict survival and immune recovery
Published in Blood (25-10-2018)“…The Primary Immune Deficiency Treatment Consortium (PIDTC) performed a retrospective analysis of 662 patients with severe combined immunodeficiency (SCID) who…”
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Excellent outcomes following hematopoietic cell transplantation for Wiskott-Aldrich syndrome: a PIDTC report
Published in Blood (04-06-2020)“…Wiskott-Aldrich syndrome (WAS) is an X-linked disease caused by mutations in the WAS gene, leading to thrombocytopenia, eczema, recurrent infections,…”
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Antiviral cellular therapy for enhancing T-cell reconstitution before or after hematopoietic stem cell transplantation (ACES): a two-arm, open label phase II interventional trial of pediatric patients with risk factor assessment
Published in Nature communications (18-04-2024)“…Viral infections remain a major risk in immunocompromised pediatric patients, and virus-specific T cell (VST) therapy has been successful for treatment of…”
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Relevance of lymphocyte proliferation to PHA in severe combined immunodeficiency (SCID) and T cell lymphopenia
Published in Clinical immunology (Orlando, Fla.) (01-04-2024)“…Severe combined immunodeficiency (SCID) is characterized by a severe deficiency in T cell numbers. We analyzed data collected (n = 307) for PHA-based T cell…”
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